1-iodo-4-decyloxybenzene | 93144-80-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 1-iodo-4-decyloxybenzene
• 英文别名: 1-decyloxy-4-iodobenzene；4-Decyloxy-iodbenzol；p-n-decyloxy-iodobenzene；1-decoxy-4-iodobenzene
• CAS: 93144-80-0
• 化学式: C₁₆H₂₅IO
• mdl: MFCD00441843
• 分子量: 360.278
• InChiKey: DVOCKTGXOLQSOR-UHFFFAOYSA-N

物化性质

• 熔点：
  21-22.5 °C
• 沸点：
  379.3±25.0 °C(Predicted)
• 密度：
  1.268±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  7.2
• 重原子数：
  18
• 可旋转键数：
  10
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.625
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  1-iodo-4-decyloxybenzene 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide 氢氧化钾 、 三乙胺 、 三苯基膦 作用下， 以 四氢呋喃 、 甲苯 为溶剂， 反应 4.0h， 生成 [4-(4'-n-decyloxyphenyl)acetylenyl]phenyl 3-fluorobenzoate
  参考文献：
  名称：

  Synthesis and Mesomorphic Properties of Some Fluoro-Substituted Benzoates

  摘要：

  Several series of fluoro-substituted benzoate liquid crystals have been synthesized. The results showed that the SmA phase is enhanced with the increasing of the degree of fluoro-substitution on the para- and meta-postion of the terminal phenyl groups. And the molecules which have same molecular structural formula show nearly the same melting points. It is also discussed about the effect of the eater bond's direction on the mesomorphic properties.

  DOI：

  10.1080/10587250008024803
• 作为产物：
  描述：

  癸基溴 、 4-碘苯酚 在 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 12.5h， 以94%的产率得到1-iodo-4-decyloxybenzene
  参考文献：
  名称：

  Dicationic imidazolium-based ionic liquids and ionic liquid crystals with variously positioned fluoro substituents

  摘要：

  合成并表征了一系列新的二阳离子咪唑盐，这些盐在弯曲核心单元和/或连接苯环位置上具有氟取代基。这些盐的性质，包括相变温度、分解温度和密度得到了测定，表明它们的性能强烈依赖于氟取代基的位置、烷基链中碳原子的数量以及所含的阴离子。通过偏光显微镜的观察显示，四种盐（化合物4c、7a、7b和8b，其中烷基链为C12H25–）具有介晶性，这些数据得到了差示扫描量热法（DSC）测量的支持。

  DOI：

  10.1039/b912873e

文献信息

• Thermal and nonlinear optical studies of newly synthesized EDOT based bent-core and hockey-stick like liquid crystals
  作者：Ashwathanarayana Gowda、Litwin Jacob、Nithin Joy、Reji Philip、Pratibha R、Sandeep Kumar

  DOI：10.1039/c7nj04807f

  日期：——

  Novel EDOT based bent-core and hockey-stick shaped mesogens bearing terminal alkyl chains and alkoxy terminal chains, respectively, have been designed and synthesized via the Sonogashira coupling reaction. Molecular structures of these new compounds were determined using spectral and elemental analysis. The mesomorphic behaviour of all the novel compounds was primarily investigated by a combination

  新型EDOT基弯曲核和曲棍球状介晶分别带有末端烷基链和烷氧基末端链，已通过设计和合成，Sonogashira偶联反应。这些新化合物的分子结构使用光谱和元素分析确定。主要通过偏振光学显微镜（POM），差示扫描量热法（DSC）和X射线衍射研究（XRD）的组合研究了所有新化合物的介晶行为。所有化合物均以较低的同系物表现出对映向列相。但是，在较高的BC和曲棍球LC同源物中观察到了较低的近晶A相和高温向列相。进行了密度泛函理论研究以研究稳定构型。这些分子的弯曲角介于钙质LC和香蕉LC之间。在无水氯仿溶剂中研究了所有化合物的光物理性质，它们在370-395 nm左右具有吸收模式，在418-465 nm之间具有发射模式。我们还报道了当在532 nm的纳秒激光脉冲激发下测量时，这些新型化合物具有较大的有效两光子吸收率。所有介晶化合物都是非线性材料，这使其成为光学限制应用的合适候选物。
• Liquid crystal compounds and compositions
  申请人：SANYO CHEMICAL INDUSTRIES, LTD.

  公开号：EP0500210A2

  公开（公告）日：1992-08-26

  Smectic C liquid crystal compounds, represented by the following formula (1) or (2) are disclosed. wherein R1 and R2 are C1-18 alkyl groups; A is a cyclic group, such as substituted or unsubstituted 1,4-phenylene group, X is direct bond, O or C-C ; Z is -C≡C- or -CH2CH2-; one of A1 and A2 is 1,4-phenylene group and the other is 2,3-difluoro-1,4-phenylene group ; and p is 0 or 1. These compounds can provide ferroelectric liquid crystal composition of low viscosity, and are useful as a component giving negative dielectric anisotropy and enlarging a temperature range showing smectic C phase.

  液晶化合物Smectic C，其化学式如下（1）或（2）所示。其中，R1和R2为C1-18烷基基团；A为环状基团，如取代或未取代的1,4-苯基基团；X为直接键，O或C-C；Z为-C≡C-或-CH2CH2-；A1和A2中的一个为1,4-苯基基团，另一个为2,3-二氟-1,4-苯基基团；p为0或1。这些化合物可以提供低粘度的铁电液晶组合物，并且可作为给出负介电各向异性并扩大显示Smectic C相的温度范围的组分。
• Helical and Flat Structures from Chiral Dendronized Rectangular Oligo(phenylene ethynylene)s
  作者：Fátima García、Fátima Aparicio、Marco Marenchino、Ramón Campos-Olivas、Luis Sánchez

  DOI：10.1021/ol101673z

  日期：2010.10.1

  The synthesis of two chiral amphiphiles and their self-assembling features in solution and onto surfaces is reported. The different degree of interdigitation of the paraffinic substituents has an enormous influence in the chirality of the aggregates. Thus, while oligo(phenylene ethynylene) 1 shows a bisignated Cotton effect in solution and P-type helices onto surfaces, compound 2 lacks in any dichroic

  报道了两种手性两亲物的合成及其在溶液中和表面上的自组装特征。链烷烃取代基的相互交叉程度不同，对聚集体的手性有很大影响。因此，尽管低聚（亚苯基亚乙炔基）1在溶液中显示出双向作用的棉花效应，并且在表面上呈现P型螺旋，但化合物2在室温下没有任何二向色性反应，并且自组装成扁平带。
• Mesogenic, optical, and dielectric properties of 5-substituted 2-[12-(4-pentyloxyphenyl)-p-carboran-1-yl] [1,3]dioxanes
  作者：Takashi Nagamine、Adam Januszko、Piotr Kaszynski、Kiminori Ohta、Yasuyuki Endo

  DOI：10.1039/b608012j

  日期：——

  Two homologous series of carborane-containing dioxanes 1[n] and 2[n] (n = 1–10) were prepared and their mesogenic properties investigated. All compounds exhibit nematic behavior and three members of series 2[n] show an E phase. Numerical analysis of the clearing temperatures gave a limiting value TNI(∞) of 89 °C for series 2[n] and indicated conformational flexibility of the dioxane ring. Investigations of three-ring derivative 1[4] gave Δn = 0.17, S = 0.53, and Δε = +0.4 ± 0.1 at 85 °C. Extrapolation of dielectric data for dilute solutions of 1[4] in 6-CHBT gave Δε = +0.4 ± 0.25 at 24 °C. Modelling of dielectric results with the Maier–Meier equation demonstrated that conformers with a higher β angle are preferred, which is consistent with conformational selection for the most elongated conformers.

  准备了两个含有碳硼烷的二噁烷同系物系列1[n]和2[n]（n = 1–10），并对它们的介晶性质进行了研究。所有化合物均表现出向列行为，而系列2[n]中的三个成员显示出E相。清晰温度的数值分析给出了系列2[n]的极限值TNI(∞)为89°C，并表明二噁烷环的构象灵活性。对三环衍生物1[4]的研究得到了Δn = 0.17，S = 0.53，以及在85°C时Δε = +0.4 ± 0.1。对1[4]在6-CHBT稀溶液中的介电数据进行外推时，在24°C得到了Δε = +0.4 ± 0.25。利用Maier–Meier方程对介电结果的建模表明，具有更高β角的构象更为偏好，这与对于最细长构象的构象选择一致。
• Optically active compounds
  申请人：Sanyo Chemical Industries, Ltd.

  公开号：US05160662A1

  公开（公告）日：1992-11-03

  Optically active compounds having the following formulae (1), (2) or (3) ##STR1## wherein R and R' are C.sub.1-20 alkyl groups; X and Y.sub.1 are --, O, S, or divalent groups such as COO, OOC and OCOO; m is 0 or 1; n is 0 to 5; A.sub.2 is a cyclic group, such as p,p'-biphenylene, 2,6-naphthylene, 2,5-pyrimidinylene-1,4-phenylene, A.sub.1 -Y.sub.2 -pyridylene or A.sub.4 -Y.sub.2 -A.sub.5 ; Y.sub.2 is CH.sub.2 CH.sub.2 or C.tbd.C; A.sub.3 is 2,6-naphthylene, A.sub.1 -Y.sub.2 -pyridylene or A.sub.6 -CH.sub.2 CH.sub.2 -A.sub.7 ; and A.sub.1, A.sub.4, A.sub.5, A.sub.6 and A.sub.7 are cyclic groups, such as 1,4-phenylene and/or 4,4'-biphenylene.

  具有以下化学式（1）、（2）或（3）的光学活性化合物 其中R和R'是C.sub.1-20烷基基团；X和Y.sub.1是--，O，S或COO，OOC和OCOO等二价基团；m为0或1；n为0至5；A.sub.2是环状基团，例如p，p'-联苯基，2,6-萘基，2,5-嘧啶基-1,4-苯基，A.sub.1 -Y.sub.2 -吡啶基或A.sub.4 -Y.sub.2 -A.sub.5；Y.sub.2是CH.sub.2 CH.sub.2或C.tbd.C；A.sub.3是2,6-萘基，A.sub.1 -Y.sub.2 -吡啶基或A.sub.6 -CH.sub.2 CH.sub.2 -A.sub.7；而A.sub.1，A.sub.4，A.sub.5，A.sub.6和A.sub.7是环状基团，例如1,4-苯基和/或4,4'-联苯基。